Primary Device ID | 06975029700061 |
NIH Device Record Key | 2d641bf8-be2c-48e0-bc66-47c9f98ea1ff |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MTEHFYAF |
Version Model Number | MY-FZS-01 |
Company DUNS | 414510435 |
Company Name | Beijing Xingjian Yongzhen Technology Co. , Ltd. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06975029700061 [Primary] |
BYW | Device, Rebreathing |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-06-20 |
Device Publish Date | 2024-06-12 |
06975029700078 | MY-QYJ-01 |
06975029700061 | MY-FZS-01 |
06975029700054 | MY-FYY-03 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MTEHFYAF 98473311 not registered Live/Pending |
Beijing Xingjian Yongzhen Technology Co. Ltd. 2024-03-28 |